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<jats:title>Key Points</jats:title> <jats:p>Twelve independent, novel, low-frequency (n = 2) and rare (n = 10) genetic variants were associated with fibrinogen, FVII, FVIII, or vWF. Nine were within previously associated genes, and 3 novel candidate genes (KCNT1, HID1, and KATNB1) were confined to cohorts of African ancestry.</jats:p>

Original publication

DOI

10.1182/blood-2015-02-624551

Type

Journal article

Journal

Blood

Publisher

American Society of Hematology

Publication Date

10/09/2015

Volume

126

Pages

e19 - e29